EP0265251A2 - Sperrschichtphotozelle mit P-I-N Übergängen des heterogenen Typs - Google Patents

Sperrschichtphotozelle mit P-I-N Übergängen des heterogenen Typs Download PDF

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Publication number
EP0265251A2
EP0265251A2 EP87309322A EP87309322A EP0265251A2 EP 0265251 A2 EP0265251 A2 EP 0265251A2 EP 87309322 A EP87309322 A EP 87309322A EP 87309322 A EP87309322 A EP 87309322A EP 0265251 A2 EP0265251 A2 EP 0265251A2
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Prior art keywords
layer
type
photovoltaic cell
intrinsic
cell according
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EP87309322A
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English (en)
French (fr)
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EP0265251A3 (en
EP0265251B1 (de
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Peter V. Meyers
Chung-Heng Liu
Timothy J. Frey
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Colorado School of Mines Foundation Inc
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Ametek Inc
Colorado School of Mines Foundation Inc
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    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F10/00—Individual photovoltaic cells, e.g. solar cells
    • H10F10/10—Individual photovoltaic cells, e.g. solar cells having potential barriers
    • H10F10/17—Photovoltaic cells having only PIN junction potential barriers
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F10/00—Individual photovoltaic cells, e.g. solar cells
    • H10F10/10—Individual photovoltaic cells, e.g. solar cells having potential barriers
    • H10F10/16—Photovoltaic cells having only PN heterojunction potential barriers
    • H10F10/162—Photovoltaic cells having only PN heterojunction potential barriers comprising only Group II-VI materials, e.g. CdS/CdTe photovoltaic cells
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F10/00—Individual photovoltaic cells, e.g. solar cells
    • H10F10/10—Individual photovoltaic cells, e.g. solar cells having potential barriers
    • H10F10/16—Photovoltaic cells having only PN heterojunction potential barriers
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F10/00—Individual photovoltaic cells, e.g. solar cells
    • H10F10/10—Individual photovoltaic cells, e.g. solar cells having potential barriers
    • H10F10/17—Photovoltaic cells having only PIN junction potential barriers
    • H10F10/174—Photovoltaic cells having only PIN junction potential barriers comprising monocrystalline or polycrystalline materials
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F71/00—Manufacture or treatment of devices covered by this subclass
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F71/00—Manufacture or treatment of devices covered by this subclass
    • H10F71/125—The active layers comprising only Group II-VI materials, e.g. CdS, ZnS or CdTe
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00—Constructional details of devices covered by this subclass
    • H10F77/10—Semiconductor bodies
    • H10F77/12—Active materials
    • H10F77/123—Active materials comprising only Group II-VI materials, e.g. CdS, ZnS or HgCdTe
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00—Constructional details of devices covered by this subclass
    • H10F77/10—Semiconductor bodies
    • H10F77/16—Material structures, e.g. crystalline structures, film structures or crystal plane orientations
    • H10F77/162—Non-monocrystalline materials, e.g. semiconductor particles embedded in insulating materials
    • H10F77/164—Polycrystalline semiconductors
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00—Constructional details of devices covered by this subclass
    • H10F77/10—Semiconductor bodies
    • H10F77/16—Material structures, e.g. crystalline structures, film structures or crystal plane orientations
    • H10F77/169—Thin semiconductor films on metallic or insulating substrates
    • H10F77/1696—Thin semiconductor films on metallic or insulating substrates the films including Group II-VI materials, e.g. CdTe or CdS
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00—Constructional details of devices covered by this subclass
    • H10F77/30—Coatings
    • H10F77/306—Coatings for devices having potential barriers
    • H10F77/311—Coatings for devices having potential barriers for photovoltaic cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/543—Solar cells from Group II-VI materials
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/547—Monocrystalline silicon PV cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/548—Amorphous silicon PV cells

Definitions

  • the present invention relates to photovoltaic cells, and more particularly to a low cost, high efficiency heterojunction p-i-n photovoltaic cell.
  • Photovoltaic cells convert visible and near visible light energy to usable direct current electricity.
  • Photovoltaic cells encompass solar cells which convert the visible and near visible light energy of the sun to usable direct current electricity.
  • the known heterojunction photovoltaic cells utilize two semiconductor materials to produce a rectifying junction.
  • the advantages of utilizing this design include the ability to choose materials with properties appropriate for each component of the device and the reduced necessity for compromise with the property requirements of other components of the device.
  • An example of this is the use of a wide band gap "window" semiconductor material of one carrier type (e.g., an n-type) as a barrier layer on a more narrow band gap "absorber" semiconductor material of the opposite carrier type (e.g., a p-type).
  • the amount of radiation absorbed (and therefore the electrical current generated in the device) increases with decreasing band gap width, while the diffusion potential obtainable within the device (and therefore the electrical voltage generated in the device) increases with band gap width.
  • the absorber material is chosen to maximize the solar radiation absorbed and afford reasonable diffusion potential, while the window material is chosen to absorb a minimum amount of solar radiation.
  • Further design considerations include consideration of the electrical conductivity, chemical stability, density of bulk and interface electron and hole traps and recombination centers, availability of suitable ohmic contacts, electron and hole (i.e., charge carrier) mobilities, electron and hole lifetimes, discontinuities in the valence and conduction bands at the interface, absorption coefficient, material cost, ease of deposition, chemical or environmental stability, preferred carrier type, and other attributes of semiconductors well known in the photovoltaic art.
  • the principle of the p-i-n structure involves the creation of a diffusion potential across a relatively wide, high resistivity intrinsic layer. This diffusion potential is generated by the p and n regions on either side of the intrinsic layer.
  • a feature of this structure is that the light is absorbed within the field region, and thus photogenerated positive and negative charge carriers are field assisted toward the p and n regions, respectively.
  • the band gap of the p or n semiconductor facing the incident radiation is increased to permit more solar radiation to be absorbed within the intrinsic layer.
  • the p-i-n structure has been utilized in both amorphous and single crystal devices. Single crystal devices have been eschewed, possibly due to the high cost of single crystal materials and the difficulty of depositing them.
  • P-i-n solar cells have been constructed of amorphous materials, but the carrier mobility and lifetime are low.
  • heterojunction cells have been analyzed using the p-i-n model, no heterojunction devices of three or more layers (i.e., heterojunction p-i-n devices) have been produced heretofore.
  • Another object is to provide such a cell in which the cost of manufacturing the same is minimized and the photovoltaic efficiency (i.e., the ratio of electrical power output to radiant power input) is maximized.
  • a further object is to provide such a cell using polycrystalline materials for some, and preferably all, of the semiconductor layers thereof.
  • a heterojunction p-i-n photovoltaic cell comprised of at least three different semiconductor layers and first and second ohmic contacts.
  • the three different semiconductor layers are formed of at least four different elements and include a p-type relatively wide band gap semiconductor layer, a high-resistivity intrinsic semiconductor layer, used as an absorber of light radiation, and an n-type relatively wide band gap semiconductor layer, the intrinsic layer being in electrically conductive contact on one side with the p-type layer and on an opposite side of the n-type layer.
  • the first and second ohmic contacts make electrical contact with the p-type layer and the n-type layer, respectively.
  • compositions of the n-type, intrinsic and p-type semiconductor layers are chosen so as to minimize spikes in the conduction band edge at the interface between the intrinsic layer and the n-type layer and the valence band edge at the interface between the intrinsic layer and the p-type layer. This is accomplished through the use of compositions for the intrinsic and p-type layers which have a common anion and (thereby to reduce spikes in the valence band) and compositions for the intrinsic and n-type layers which have a common cation (thereby to minimize spikes in the conduction band).
  • One or more intermediate layers may be disposed between the intrinsic layer and one, or both, of the p-type and n-type layers, the intrinsic layer being in electrically conductive contact with the one layer through the one or more intermediate layers.
  • the semiconductor layers are polycrystalline and II-VI compounds.
  • the p-type layer is ZnTe
  • the intrinsic layer is CdTe
  • the n-type layer is CdS.
  • the n-type layer is CdS deposited by vacuum evaporation or, preferably, in a narrow gap reactor, the intrinsic layer is electrodeposited CdTe and the p-type layer is vacuum evaporation deposited ZnTe.
  • the n-type layer is preferably deposited onto a transparent substrate comprising a transparent conducting oxide layer and a glass plate supporting the oxide layer, the oxide layer electronically connecting the n-type layer and the second ohmic contact.
  • n-type and p-type layers are preferably devoid of common anions and common cations.
  • the cells of the present invention may achieve efficiencies greater than 10%.
  • Layers are sectioned in FIGS. 2-4 to indicate non-transparency to the incident light.
  • FIG. 1 therein illustrated is a schematic energy band diagram for a heterojunction p-i-n photovoltaic cell, such as those illustrated in FIGS. 2-4 and generally designated by the reference numerals 10, 10 ⁇ , and 10 ⁇ , respectively.
  • the energy band diagram is a plot of the electron energy against the depth of the cell, in conventional fashion.
  • FIG. 2 wherein there is illustrated the first embodiment of a heterojunction p-i-n photovoltaic cell according to the present invention, generally designated by the reference numeral 10.
  • the photovoltaic cell 10 which may find utility as a solar cell, is comprised of at least three different semiconductor layers and two ohmic contacts.
  • the semiconductor layers are together composed of at least four different elements (exclusive of dopants) and include a p-type relatively wide band gap semiconductor layer 12, a high resistivity intrinsic semiconductor layer 14 used as an absorber of light radiation, and an n-type relatively wide band gap semiconductor layer 16.
  • the p-type and n-type layers 12 and 16 are relatively wide band gap "window" layers relative to the narrow band gap "absorber" intrinsic layer.
  • the intrinsic layer has an upper surface in electrically conductive contact with the p-type layer 12 and a bottom surface in electrically conductive contact with the n-type layer 16.
  • the ohmic contacts 20 and 22 are in electrically conductive contact with the p-type and n-type layers 12 and 16, respectively.
  • the term "ohmic contact,” as used herein, refers to materials and structures which produce a low resistance junction with the relevant semiconductor material and allow current to pass freely into an external electrical circuit. It is anticipated that one or more intermediate layers may be required in order to more fully realize the benefits of this device. For example, intermediate layers might be inserted between either electrical contact 20 or 22 and semiconductor layers 12 or 16 in order to improve the quality of the contact, such as by passivating the semiconductor surface 12, 16, by reducing the contact resistance, or by increasing the physical or chemical stability of the interface.
  • the three semiconductor layers 12, 14, and 16 are preferably each polycrystalline in nature, such polycrystalline materials frequently being cheaper and more easily deposited than single crystalline materials affording greater carrier mobility and lifetime than amorphous materials.
  • amorphous and single crystalline materials are useful in the practice of the present invention, the polycrystalline materials are preferred.
  • the semiconductor layers 12, 14, and 16 are formed of the II-VI compounds well known for their utility in photovoltaic applications. While binary compounds are preferred, ternary compounds may also be used. More specifically, in the preferred embodiment ZnTe is employed as the p-type layer 12, CdTe as the intrinsic layer 14, and CdS as the n-type layer 16. Advantages of this specific configuration include the fact that CdS prefers to be n-type, ZnTe prefers to be p-type, and CdTe is self-compensating and thus prefers to be intrinsic. The intrinsic layer of CdTe may be electrodeposited on either the p-type layer or the n-type layer. The four different elements in these three semiconductor layers are Zn, Te, Cd and S.
  • this embodiment has the advantage that n-type carriers (electrons) are reflected from the p-type layer by the discontinuity in the conduction band edge at the interface between the intrinsic and p-type layers, and that p-type carriers (holes) are reflected from the n-type layer by the discontinuity in the valence band edge at the junction between the intrinsic and n-type layers.
  • This reflection has the effect of reducing the number of holes and electrons reaching the n-type and p-type regions, respectively, thus reducing the number of charge carriers lost via recombination in the n-type and p-type layers.
  • binary compound semiconductors often utilize compounds with at least one element in common on each side of the junction. Such binary compounds with a common cation would be expected to have a minimal discontinuity in the conduction band, while, such binary compounds with a common anion would be expected to have a minimal discontinuity in the valence band.
  • the p-i-n device 10 utilizes a common anion in the valence band edge between the intrinsic and p-type layers and a common cation in the conduction band edge between the intrinsic and n-type layers.
  • the p-type layer and n-type layers share neither a common anion nor a common cation.
  • the interfaces between adjacent layers are depicted as abrupt in FIG. 1 and 2, it is expected that real junctions may have a measurable width. Thus it is possible that some interdiffusion will occur at some time during device fabrication or use. This is to be expected especially in the case of junctions consisting of II-VI compound semiconductors which often form solid solutions.
  • the compounds ZnTe and CdTe may be viewed as the end points of the solid solution Cd 1-x Zn x Te at which x attains its limiting values of 1 and 0, respectively.
  • the solid solution CdS 1-x Te x is known to exist in a continuum of stable compositions. The situation is similar for other compounds. Thus, many variations are possible, and the existence of graded interfaces is to be expected. The meris of such intentionally interdiffused interfaces are not known; however, it is possible that the degree of interdiffusion will affect, and possibly improve, the electrical, optical and chemical properties of the device.
  • interface states may have no effect on the operation of a solar cell; in other instances they may even be beneficial.
  • interface states are detrimental to the efficient operation of a solar cell. For example, interface states may become charged and thereby decrease the magnitude of the voltage drop, and therefore the penetration of the space charge region, within the absorber semiconductor. This has the effect of reducing both the current and the voltage generated by the solar cell.
  • the interface states may serve as recombination centers for minority charge carriers with majority charge carriers, thus reducing the number of photogenerated carriers collected and therefore the current generated by the solar cell.
  • This passivation may be accomplished by growing or depositing an intermediate layer at the interface between the two semiconductor materials.
  • This intermediate layer might, for example, be composed of an oxide grown onto one of the semiconductors, i.e, a native oxide.
  • the intermediate layer might be a compound with no elements in common with either semiconductor material.
  • the application of such passivation layers is well known in the photovoltaic art.
  • intermediate layers may be inserted between the intrinsic layer 14 and either or both of layers 12 and 16 for the purpose of passivating the interfaces therebetween, or of improving the electrical or optical coupling between layers, or of increasing the chemical or physical stability of the interface.
  • an anti-reflection coating 18 may be applied to the upper surface of the p-type layer 12 in order to increase the amount of light entering the device.
  • a current collecting grid 24 on top of the p-type layer 12 is employed as part of the ohmic contact 20 and a conducting layer 26 below the n-type layer 16 is part of the ohmic contact 22.
  • the conducting layer 26 is non-transparent although a transparent layer could be employed if desired.
  • the device (and in particular conducting layer 26) is supported on a substrate 28 which, if desired, may serve as both physical support and as part of the ohmic contact 22.
  • FIG. 3 therein illustrated is a second embodiment of the present invention, generally designated by the reference numeral 10 ⁇ , wherein the light is incident through the n-type layer 16.
  • the three semiconductor layers are in reverse order from the first embodiment 10, with the n-type layer 16 on top, the intrinsic layer 14 therebelow, and the p-type layer 12 at the bottom.
  • the current collecting grid 24 is a component of the ohmic contact 22 in conductive contact with the n-type layer 16 and the non-transparent conducting layer 26 is part of the ohmic contact 20 in conductive contact with the p-type layer 12.
  • the anti-reflection layer 18 is, of course, on top of the exposed upper surface of the n-type layer 16 rather than the p-type layer 12.
  • FIG. 4 therein illustrated is a third embodiment of the present invention, generally designated by the reference numeral 10 ⁇ .
  • the third embodiment 10 ⁇ is similar to the first embodiment 10 except that the conductive grid 24 is replaced by a continuous conducting layer 30 as part of the ohmic contact 20 to the p-type layer 12, and the ohmic conducting layer 26 is replaced by a transparent conducting layer 32 as part of the ohmic contact 22 to the n-type layer 16.
  • the substrate 28 which in the first and second embodiments could, but need not be transparent, is necessarily transparent as the light is incident on the n-type layer 16 through the substrate 28 and conducting layer 32. If desired, an anti-reflection layer may be deposited on the exposed bottom face of the substrate layer 28.
  • the ohmic contact 30 to the p-type layer is formed of a material transparent to light of wavelength greater than that absorbed by the intrinsic layer 14. This allows a significant fraction of the radiant energy to pass through the device. This transmitted energy is then available for other applications. Specifically the p-i-n device may then operate as the top cell in a cascade solar cell. Another lower band gap solar cell placed behind the top cell would then produce additional electrical energy, thus increasing the overall efficiency of the sunlight-to-electricity conversion.
  • an ultrasonically cleaned low-sodium, borosilicate glass slide is coated with a transparent oxide front coating such as indium-tin-oxide or tin oxide.
  • the CdS film is deposited on the coated glass substrate, for example, by vacuum deposition or by a narrow reaction gap process (as described in co-pending U.S. Patent Application Serial No. 863,929, filed May 15, 1986).
  • the vacuum deposited layer may be about 1 ⁇ m while the narrow reaction gap process deposited layer is about 1500 ⁇ .
  • CdTe is electrodeposited from an aqueous bath containing cadmium and tellurium ions using techniques fully described in U.S. Patent No. 4,260,427.
  • the composite structure is then heat treated, and the CdTe is given a bromine-methanol etching rinse to prepare it for ZnTe deposition.
  • a further preparation of the surface may be effected by soaking it in a sodium sulfate/potassium hydroxide solution and rinsing it in deionized water.
  • ZnTe is evaporated in a vacuum onto the rinsed surface to the desired thickness (for example, .06 ⁇ m to 0.15 ⁇ m).
  • vacuum evaporated gold, indium- tin-oxide or a combination of either with silver-impregnated epoxy may be used as the ohmic back contact to the p-type layer of ZnTe.
  • the ohmic contact 20 in conductive contact with the p-type layer 12 may be gold, a silver-containing epoxy, an indium-tin-oxide component or like materials, depending on the intended application.
  • the ohmic contact 22 in conductive contact with the n-type layer 16 may be tin oxide, indium-tin-oxide, a silver-containing epoxy or like materials.
  • a cell was prepared as in Example I except that silver-impregnated epoxy was applied both to the gold contact in order to reduce the sheet resistance of the back contact and to the SnO2 surrounding the cell in order to reduce the series resistance of the front contact.
  • a cell was prepared as in Example II with the following exceptions:
  • the optical transmission at 900 nm was 32%, an important property where the cell is to be used as part of a cell cascade.
  • a cell was prepared as in Example II with the following exceptions:
  • the present invention combines a minimization of cost of manufacture with a maximization of efficiency.
  • Minimization of cost is achieved by the use of thin films (less than 10 microns thick) of selected component materials and by an efficient manufacturing process. More particularly, the use of II-VI compounds as component materials provides not only relatively low material cost, but also ease of deposition of the semiconductor layers.
  • Maximization of efficiency is achieved by the proper selection of materials and the design of the photovoltaic cell. The materials are selected to minimize energy band discontinuities or spikes at the interfaces between semiconductors, and the cell design utilizes concepts which are known to produce efficient cells--namely, the p-i-n structure and the heterojunction interface.
  • a high optical transmission level enables use of the cell in a cascade; in other particular embodiments an efficiency in excess of 10% is achieved.

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  • Photovoltaic Devices (AREA)
EP87309322A 1986-10-21 1987-10-21 Sperrschichtphotozelle mit P-I-N Übergängen des heterogenen Typs Expired - Lifetime EP0265251B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US922122 1986-10-21
US06/922,122 US4710589A (en) 1986-10-21 1986-10-21 Heterojunction p-i-n photovoltaic cell

Publications (3)

Publication Number Publication Date
EP0265251A2 true EP0265251A2 (de) 1988-04-27
EP0265251A3 EP0265251A3 (en) 1989-04-26
EP0265251B1 EP0265251B1 (de) 1995-03-08

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EP87309322A Expired - Lifetime EP0265251B1 (de) 1986-10-21 1987-10-21 Sperrschichtphotozelle mit P-I-N Übergängen des heterogenen Typs

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US (1) US4710589A (de)
EP (1) EP0265251B1 (de)
JP (1) JP2702129B2 (de)
KR (1) KR960004097B1 (de)
AT (1) ATE119712T1 (de)
AU (1) AU604509B2 (de)
CA (1) CA1299715C (de)
DE (1) DE3751133D1 (de)
IL (1) IL84217A (de)
ZA (1) ZA877875B (de)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0266050A3 (en) * 1986-10-31 1989-04-26 The Standard Oil Company Improved photovoltaic heterojunction structures
US8076175B2 (en) 2008-02-25 2011-12-13 Suniva, Inc. Method for making solar cell having crystalline silicon P-N homojunction and amorphous silicon heterojunctions for surface passivation

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4873198A (en) * 1986-10-21 1989-10-10 Ametek, Inc. Method of making photovoltaic cell with chloride dip
US4977097A (en) * 1986-10-21 1990-12-11 Ametek, Inc. Method of making heterojunction P-I-N photovoltaic cell
US4764261A (en) * 1986-10-31 1988-08-16 Stemcor Corporation Method of making improved photovoltaic heterojunction structures
EP0296371B1 (de) * 1987-06-22 1992-12-23 Landis & Gyr Business Support AG Photodetektor für Ultraviolett und Verfahren zur Herstellung
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CA1299715C (en) 1992-04-28
EP0265251A3 (en) 1989-04-26
DE3751133D1 (de) 1995-04-13
ZA877875B (en) 1988-06-29
US4710589A (en) 1987-12-01
EP0265251B1 (de) 1995-03-08
AU8001487A (en) 1988-04-28
KR960004097B1 (ko) 1996-03-26
ATE119712T1 (de) 1995-03-15
JP2702129B2 (ja) 1998-01-21
IL84217A0 (en) 1988-03-31
AU604509B2 (en) 1990-12-20
IL84217A (en) 1992-01-15
JPS63110777A (ja) 1988-05-16
KR880005701A (ko) 1988-06-30

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